| Identification | More | [Name]
(S)-(-)-2-AMINO-1,1-DIPHENYL-1-PROPANOL | [CAS]
78603-91-5 | [Synonyms]
1,1-DIPHENYL-L-ALANINOL
(S)-(-)-2-AMINO-1,1-DIPHENYL-1-PROPANOL
(S)-2-AMINO-1,1-DIPHENYL-1-PROPANOL
(S)-2-AMINO-1,2-DIPHENYL-1-PROPANOL
(2S)-2-amino-1,1-diphenylpropan-1-ol
(-)-[(S)-1-Aminoethyl]diphenylmethanol
(-)-α-(1-Aminoethyl)benzhydrol
(2S)-1,1-Diphenyl-2-amino-1-propanol
(S)-1,1-Diphenyl-2-amino-1-propanol | [EINECS(EC#)]
622-109-8 | [Molecular Formula]
C15H17NO | [MDL Number]
MFCD00145253 | [Molecular Weight]
227.3 | [MOL File]
78603-91-5.mol |
| Chemical Properties | Back Directory | [Appearance]
white to light yellow crystal powde | [Melting point ]
100-102 °C(lit.)
| [alpha ]
-90 º (C=1 IN CHLOROFORM) | [Boiling point ]
407.8±40.0 °C(Predicted) | [density ]
1.112±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
solid | [pka]
11.25±0.50(Predicted) | [color ]
Yellow | [Optical Rotation]
[α]20/D 90°, c = 1 in chloroform | [BRN ]
3052863 | [InChI]
InChI=1/C15H17NO/c1-12(16)15(17,13-8-4-2-5-9-13)14-10-6-3-7-11-14/h2-12,17H,16H2,1H3/t12-/s3 | [InChIKey]
FMBMNSFOFOAIMZ-PLAQIDKDNA-N | [SMILES]
C(O)([C@@H](N)C)(C1C=CC=CC=1)C1C=CC=CC=1 |&1:2,r| | [CAS DataBase Reference]
78603-91-5(CAS DataBase Reference) |
| Questions And Answer | Back Directory | [Uses]
(S)-2-amino-1,1-diphenyl-1-propanol is an alcohol derivative that can be used as an intermediate in organic synthesis. | [Application]
In asymmetric synthesis, the synthesis of chiral catalysts or chiral auxiliaries is crucial. Chiral amino alcohols are widely used as ligands or catalysts for catalyzing asymmetric synthetic reactions and are also important precursors for the synthesis of many chiral drugs, natural products, and chemical and biological functional materials. (S)-2-amino-1,1-diphenyl-1-propanol belongs to the optically active β-amino alcohols. It can be used for asymmetric reduction of pre-chiral ketones, asymmetric catalytic epoxidation reactions, and asymmetric catalytic alkylation reactions of carbonyl compounds. (S)-2-amino-1,1-diphenyl-1-propanol has also been reported as an intermediate in the synthesis of chiral complexes in asymmetric cyclopropanation reactions. |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [F ]
9 | [HS Code ]
2922190090 |
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